About 9 results found for searched term "59-43-8" (0.056 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M6112 | Thiamine chloride | Vitamin |
| Vitamin B1 | ||
| Thiamine chloride —the biologically active form of vitamin B1—is vital for all cellular life because it is a co-factor for several essential enzymes. | ||
| M6141 | NIBR189 | GPR/FFAR |
| NIBR189 is a small molecule antagonist of the Epstein-Barr virus-induced gene 2 (EBI2; GPR183) receptor with IC50 of 16 nM(Binding) and 11 nM (Functional). | ||
| M9091 | A-779 | Angiotensin Receptor |
| A779 | ||
| A-779 is a specific antagonist of G-protein coupled receptor (Mas receptor). | ||
| M14882 | Ibrutinib-biotin | BTK |
| Ibrutinib-biotin is a probe that consists of Ibrutinib linked to biotin via a long chain linker, extracted from patent WO2014059368A1 Compound 1-5, has an IC50 of 0.755-1.02 nM for BTK. | ||
| M17574 | Pteroside D | Sesquiterpenoids |
| Pteroside D | ||
| M28650 | BRD0209 | GSK-3 |
| BRD0209 is a potent, selective and dual inhibitor of GSK3α/β inhibitor (GSK3α IC50 = 19 nM; GSK3β IC50 = 5 nM). BRD0209 is also a reversible ATP-competitive inhibitor with fast-off kinetics (Ki = 4.2 nM, respectively). BRD0209 is a tricyclic pyrazolotetrahydroquinolinone compound. BRD0209 has the potential for the research of mood disorder diseases. | ||
| M41291 | JNJ-1013 | IRAK |
| JNJ-1013 is a potent and selective IRAK1 degrader with an IC50s of 72, 443, 1071 nM for IRAK1, IRAK4, VHL FP respectively. | ||
| M50411 | Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH | Src-bcr-Abl |
| Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH is a high-affinity pentapeptide to bind to the src SH2 domain (IC50≈1 µM). | ||
| M53008 | Ala5-Galanin (2-11) | Neuropeptide Receptor |
| Ala5-Galanin (2-11) is a galanin receptor 2 (GAL2R) specific agonist with a Ki of 258 nM. | ||
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